20 Results for "

PKCζ

" in MedChemExpress (MCE) Product Catalog:
Products (20)

20 Results for "PKCζ" in MCE Product Catalog:

  • Isoforms Recommended:
86
86 Publications Verification
Cat. No.: HY-13689
CAS No.: 133053-19-7
Purity:  99.32%
Synonyms: Gö 6983; Goe 6983
Target:  

PKC

Research Areas:  

Cancer

Go 6983 is a pan-PKC inhibitor against for PKCα, PKCβ, PKCγ, PKCδ and PKCζ with IC50 of 7 nM, 7 nM, 6 nM, 10 nM and 60 nM, respectively.
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3
3 Cited Publications
Cat. No.: HY-123979
CAS No.: 3316-02-7
Purity:  95.05%
Synonyms: NSC37044
Target:  

PKC Apoptosis

Research Areas:  

Cancer

ζ-Stat (NSC37044) is a specific and atypical PKC-ζ inhibitor, with an IC50 of 5 μM. ζ-Stat can reduce melanoma cell lines proliferation and induce apoptosis, and has antitumor activity in vitro .
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3
3 Cited Publications
Cat. No.: HY-123979A
CAS No.: 31894-34-5
Purity:  ≥97.0%
Synonyms: NSC37044 trisodium
Target:  

PKC Apoptosis

Research Areas:  

Cancer

ζ-Stat trisodium (NSC37044 trisodium) is a specific and atypical PKC-ζ inhibitor, with an IC50 of 5 μM. ζ-Stat trisodium can reduce melanoma cell lines proliferation and induce apoptosis, and has antitumor activity in vitro .
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Cat. No.: HY-13626
CAS No.: 196497-48-0
Purity:  ≥99.0%
Synonyms: ES-285
Spisulosine (ES-285) is an antiproliferative (antitumoral) compound of marine origin. Spisulosine inhibits the growth of the prostate PC-3 and LNCaP cells through intracellular ceramide accumulation and PKCζ activation. Spisulosine induces apoptosis in PC-3 and LNCaP cells .
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Cat. No.: HY-18713
CAS No.: 1438881-19-6
Target:  

PKC ROCK

CRT0066854 is a potent and selective atypical PKC isoenzymes inhibitor. CRT0066854 is against full-length (FL) PKCι, PKCζ, and ROCK-II kinases with IC50 values of 132 nM, 639 nM, and 620 nM, respectively .
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Cat. No.: HY-120497
CAS No.: 1132609-87-0
Purity:  98.11%
Target:  

PKC CDK

Research Areas:  

Inflammation/Immunology

PKCζ-IN-1 is a PKCζ-selective inhibitor with an IC50 of 5.18 nM against human PKCζ. PKCζ-IN-1 also inhibits CDK2 with an IC50 of 1.04 μM. PKCζ-IN-1 is applicable to research related to immune and inflammatory diseases .
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Cat. No.: HY-18713A
CAS No.: 2250019-91-9
Target:  

PKC ROCK

Research Areas:  

Neurological Disease

CRT0066854 hydrochloride is a potent and selective atypical PKCs inhibitor. CRT0066854 is against full-length (FL) PKCι, PKCζ, and ROCK-II kinases with IC50 values of 132 nM, 639 nM, and 620 nM, respectively .
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Cat. No.: HY-117366
CAS No.: 2083630-26-4
Purity:  ≥99.0%
Target:  

PKC

Research Areas:  

Cancer

PS432 is a PKC inhibitor with IC50s of 16.9 μM (PKCι) and 18.5 μM (PKCζ), respectively. PS432 effectively inhibits the proliferation of non-small cell lung cancer cells (NSCLCs) and tumor growth in mouse xenograft models .
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Cat. No.: HY-P3012
CAS No.: 107200-92-0
Cathepsin G is a pH-dependent serine protease. Cathepsin G hydrolyzes diverse synthetic and protein substrates and remodels extracellular matrix. Cathepsin G exerts immunomodulatory effects via recruiting phagocytes, enhancing T cell motility, activating ERK1/2 and p38 MAPK signaling, and mediating PKCζ membrane translocation. Cathepsin G regulates inflammatory responses by cleaving inflammatory mediators. Cathepsin G participates in vascular regulation by converting angiotensin I to angiotensin II. Cathepsin G induces PAR4-dependent platelet activation, facilitates platelet-neutrophil aggregation, and mediates VITT-related NETosis, thrombus formation. Cathepsin G can be used for the research of immune thrombotic thrombocytopenia, cardiovascular disease, and select autoimmune and inflammatory diseases .
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Cat. No.: HY-125953
CAS No.: 477243-06-4
Synonyms: Ceramide (Egg, Chicken)
Ceramide (Egg) (Ceramide (Egg, Chicken)) is a ceramide from chicken. Ceramide (Egg) is a sphingomyelin signaling pathway second messenger. Ceramide (Egg) activates PP2A, JNK, p38 MAPK, CAPK, ceramide-activated protein phosphatase, Vav, PKCζ, and SAPK/JNK cascade. Ceramide (Egg) downregulates or inhibits AKT, survivin, CDK2, mTOR, and FLIP. Ceramide (Egg) mediates apoptosis, autophagy, cell cycle arrest, mitochondrial dysfunction, redox state shifts, and ROS generation. Ceramide (Egg) can be used for the research of cancer and neurological disease .
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Cat. No.: HY-P3818
CAS No.: 813416-46-5
Target:  

PKC

Research Areas:  

Others

PKCδ Peptide Substrate is a highly selective peptide substrate targeting PKCδ. PKCδ Peptide Substrate can only be efficiently catalyzed for phosphorylation modification by PKCδ, and Thr431 is the sole phosphorylation site. PKCδ Peptide Substrate binds to the catalytic pocket of PKC in a competitive manner, but exhibits no PKC agonistic or inhibitory activity. PKCδ Peptide Substrate is a dedicated biochemical probe for the quantitative detection of PKCδ in vitro, and can be used for studies on PKCδ-related pathways .
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Cat. No.: HY-N9097
CAS No.: 122001-32-5
Niazirin is an orally active antioxidant. Niazirin can be isolated from Moringa oleifera Lam. Niazirin reduces the production levels of ROS and MDA, while increasing the levels of superoxide dismutase SOD and glutathione peroxidase GPx. Niazirin also abolishes high glucose-induced PKCζ activation and inhibits Nox4 protein expression. Niazirin exhibits excellent free radical scavenging activity. Niazirin significantly inhibits high glucose-induced proliferation of vascular smooth muscle cells. Niazirin can be used in the research of diabetic atherosclerosis .
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Cat. No.: HY-13689R
CAS No.: 133053-19-7
Synonyms: Gö 6983 (Standard); Goe 6983 (Standard)
Target:  

PKC Reference Standards

Research Areas:  

Cancer

Go 6983 (Standard) is the analytical standard of Go 6983. This product is intended for research and analytical applications. Go 6983 is a pan-PKC inhibitor against for PKCα, PKCβ, PKCγ, PKCδ and PKCζ with IC50 of 7 nM, 7 nM, 6 nM, 10 nM and 60 nM, respectively.
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Cat. No.: HY-124308
CAS No.: 1221964-50-6
Target:  

PKC

Research Areas:  

Cancer

PS315, a derivative of PS48 (HY-15967), is an allosteric PKC inhibitor by binding to the PIF-pocket of aPKC and inducing a displacement of the active site residue Lys111. PS315 inhibits the full-length and catalytic domain constructs of PKCζ (IC50=10 μM) and PKCη (IC50=30 μM). PS315 has anti-cancer activity .
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Cat. No.: HY-P1372
Target:  

PKC

Research Areas:  

Others

PKC ζ pseudosubstrate, a PKC ζ inhibitor peptide, can be attached to cell permeabilization vector peptide .
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Cat. No.: HY-P3201
CAS No.: 799764-07-1
Target:  

Pyruvate Kinase

Research Areas:  

Neurological Disease

PKCζ/ι pseudosubstrate inhibitor has broad-spectrum effects on the PKC enzyme family and can induce memory impairment .
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Cat. No.: HY-E70855
Target:  

PKC

Research Areas:  

Cancer

PKCζ is a member of the atypical PKC subfamily and has been widely implicated in the regulation of cellular functions. The major activation pathway of PKCζ depends on phosphatidylinositol (PI)-3,4,5-trisphosphate (PIP(3)), which is mainly produced by PI-3 kinase. PKCζ Recombinant Human Active Protein Kinase is a recombinant PKCζ protein that can be used to study PKCζ-related functions .
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Cat. No.: HY-208740
CAS No.: 2488951-93-3
Target:  

PKC

Research Areas:  

Inflammation/Immunology

PKCζ-IN-2 is an orally active, selective PKCζ inhibitor with an IC50 of 0.1 nM. As an anti-inflammatory agent, PKCζ-IN-2 reduces joint swelling and ameliorates disease progression in a mouse collagen-induced arthritis model. PKCζ-IN-2 can be used for the research of rheumatoid arthritis .
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Cat. No.: HY-13626S
CAS No.: 1246298-31-6
Purity:  ≥99.0%
Synonyms: ES-285-d3
Spisulosine-d3 (ES-285-d3) is deuterium labeled Spisulosine (HY-13626). Spisulosine is an antiproliferative (antitumoral) compound of marine origin. Spisulosine inhibits the growth of the prostate PC-3 and LNCaP cells through intracellular ceramide accumulation and PKCζ activation. Spisulosine induces apoptosis in PC-3 and LNCaP cells .
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Cat. No.: HY-P3818A
Target:  

PKC

Research Areas:  

Others

PKCδ Peptide Substrate acetate is a highly selective peptide substrate targeting PKCδ. PKCδ Peptide Substrate acetate can only be efficiently catalyzed for phosphorylation modification by PKCδ, and Thr431 is the sole phosphorylation site. PKCδ Peptide Substrate acetate binds to the catalytic pocket of PKC in a competitive manner, but exhibits no PKC agonistic or inhibitory activity. PKCδ Peptide Substrate acetate is a dedicated biochemical probe for the quantitative detection of PKCδ in vitro, and can be used for studies on PKCδ-related pathways .
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